ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1760-110_1760-108dup

dbSNP: rs587779109
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000076271 SCV000107296 likely benign Lynch syndrome 2013-09-05 reviewed by expert panel research Intronic substitution with no effect on splicing, tested with NMD inhibitor
GeneDx RCV001723647 SCV001950814 benign not provided 2019-03-10 criteria provided, single submitter clinical testing

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